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PUBMED FOR HANDHELDS

Journal Abstract Search


136 related items for PubMed ID: 9628281

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  • 5. HLA DRB1, DQB1 and insulin promoter VNTR polymorphisms: interactions and the association with adult-onset diabetes mellitus in Czech patients.
    Cejkova P, Novota P, Cerna M, Kolostova K, Novakova D, Kucera P, Novak J, Andel M, Weber P, Zdarsky E.
    Int J Immunogenet; 2008 Apr; 35(2):133-40. PubMed ID: 18279373
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  • 6. Meta-analysis of the IPF1 D76N polymorphism in a worldwide type 2 diabetes population.
    Gragnoli C, Cronsell J.
    Minerva Med; 2007 Jun; 98(3):163-6. PubMed ID: 17592437
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  • 10. Polymorphism R25P in the gene encoding transforming growth factor-beta (TGF-beta1) is a newly identified risk factor for proliferative diabetic retinopathy.
    Beránek M, Kanková K, Benes P, Izakovicová-Hollá L, Znojil V, Hájek D, Vlková E, Vácha J.
    Am J Med Genet; 2002 May 15; 109(4):278-83. PubMed ID: 11992481
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  • 12. An infant with combination gene mutations for Monogenic Diabetes of Youth (MODY) 2 and 4, presenting with Diabetes Mellitus Requiring Insulin (DMRI) at 8 months of age.
    Odem J, Munzinger E, Violand S, Van Morlan A, Rife D, Bachrach B.
    Pediatr Diabetes; 2009 Dec 15; 10(8):550-3. PubMed ID: 19515026
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  • 15. Time of onset of non-insulin-dependent diabetes mellitus and genetic variation in the beta 3-adrenergic-receptor gene.
    Walston J, Silver K, Bogardus C, Knowler WC, Celi FS, Austin S, Manning B, Strosberg AD, Stern MP, Raben N.
    N Engl J Med; 1995 Aug 10; 333(6):343-7. PubMed ID: 7609750
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  • 17. IKBL promoter polymorphism is strongly associated with resistance to type 1 diabetes in Japanese.
    Yamashita T, Hamaguchi K, Kusuda Y, Kimura A, Sakata T, Yoshimatsu H.
    Tissue Antigens; 2004 Mar 10; 63(3):223-30. PubMed ID: 14989711
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  • 18. Tumour necrosis factor-alpha gene promoter polymorphism and decreased insulin resistance.
    Day CP, Grove J, Daly AK, Stewart MW, Avery PJ, Walker M.
    Diabetologia; 1998 Apr 10; 41(4):430-4. PubMed ID: 9562347
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  • 19. Pancreatic agenesis attributable to a single nucleotide deletion in the human IPF1 gene coding sequence.
    Stoffers DA, Zinkin NT, Stanojevic V, Clarke WL, Habener JF.
    Nat Genet; 1997 Jan 10; 15(1):106-10. PubMed ID: 8988180
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